Monoligated Pd(0)-catalyzed intramolecular ortho- and para-arylation of phenols for the synthesis of aporphine alkaloids. Synthesis of (−)-lirinine
Author:
Funder
Harvard NeuroDiscovery Center
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference58 articles.
1. Synthesis of (±)-aporphine utilizing Pictet–Spengler and intramolecular phenol ortho-arylation reactions
2. Intramolecular ortho-arylation of phenols utilized in the synthesis of the aporphine alkaloids (±)-lirinidine and (±)-nuciferine
3. Total Synthesis of Pradimicinone, the Common Aglycon of the Pradimicin–Benanomicin Antibiotics
4. Regioselective Arylation Reactions of Biphenyl-2-ols, Naphthols, and Benzylic Compounds with Aryl Halides under Palladium Catalysis
5. Palladium-Catalyzed Regioselective Mono- and Diarylation Reactions of 2-Phenylphenols and Naphthols with Aryl Halides
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